Lubin Joseph H, Martinusen Samantha G, Zardecki Christine, Olivas Cassandra, Bacorn Mickayla, Balogun MaryAgnes, Slaton Ethan W, Wu Amy Wu, Sakeer Sarah, Hudson Brian P, Denard Carl A, Burley Stephen K, Khare Sagar D
Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
Institute for Quantitative Biomedicine, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
bioRxiv. 2023 Jan 31:2023.01.30.526101. doi: 10.1101/2023.01.30.526101.
Although the rapid development of therapeutic responses to combat SARS-CoV-2 represents a great human achievement, it also demonstrates untapped potential for advanced pandemic preparedness. Cross-species efficacy against multiple human coronaviruses by the main protease (MPro) inhibitor nirmatrelvir raises the question of its breadth of inhibition and our preparedness against future coronaviral threats. Herein, we describe sequence and structural analyses of 346 unique MPro enzymes from all coronaviruses represented in the NCBI Virus database. Cognate substrates of these representative proteases were inferred from their polyprotein sequences. We clustered MPro sequences based on sequence identity and AlphaFold2-predicted structures, showing approximate correspondence with known viral subspecies. Predicted structures of five representative MPros bound to their inferred cognate substrates showed high conservation in protease:substrate interaction modes, with some notable differences. Yeast-based proteolysis assays of the five representatives were able to confirm activity of three on inferred cognate substrates, and demonstrated that of the three, only one was effectively inhibited by nirmatrelvir. Our findings suggest that comprehensive preparedness against future potential coronaviral threats will require continued inhibitor development. Our methods may be applied to candidate coronaviral MPro inhibitors to evaluate in advance the breadth of their inhibition and identify target coronaviruses potentially meriting advanced development of alternative countermeasures.
尽管针对抗击严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的治疗反应迅速发展是一项伟大的人类成就,但这也显示出在大流行防范方面尚未开发的潜力。主要蛋白酶(MPro)抑制剂奈玛特韦对多种人类冠状病毒的跨物种疗效引发了其抑制广度以及我们应对未来冠状病毒威胁的准备情况的问题。在此,我们描述了来自NCBI病毒数据库中所有冠状病毒的346种独特MPro酶的序列和结构分析。这些代表性蛋白酶的同源底物是从它们的多蛋白序列推断出来的。我们根据序列同一性和AlphaFold2预测的结构对MPro序列进行聚类,显示出与已知病毒亚种大致对应。与推断的同源底物结合的五种代表性MPro的预测结构在蛋白酶:底物相互作用模式上显示出高度保守性,但也有一些显著差异。对这五种代表性酶进行的基于酵母的蛋白水解分析能够证实其中三种对推断的同源底物具有活性,并表明在这三种中,只有一种能被奈玛特韦有效抑制。我们的研究结果表明,针对未来潜在的冠状病毒威胁进行全面防范将需要持续开发抑制剂。我们的方法可应用于候选冠状病毒MPro抑制剂,以预先评估其抑制广度,并确定可能值得进一步开发替代对策的目标冠状病毒。